View drug registration information details.
| Items | Registration information |
|---|
| ID | 481 |
|---|
| No | 481 |
|---|
| Brand Name | CYPRESS |
|---|
| Ingredients | CYPROTERONE ACETATE PH.EUR 2 MG, ETHINYLESTRADIOL PH.EUR 0.035 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU/PVDC |
|---|
| Storage | STORE BELOW 30C |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | A BLISTERPACK OF 21 TABLETS |
|---|
| Dispensing Category | PRESCRIPTION |
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| ATC Classification | G03HB01 |
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| Pharmaceutical Class | ANTIANDROGEN |
|---|
| Indications | TREATMENT OF MODERATE TO SEVERE ACNE RELATED TO ANDROGEN-SENSITIVITY (WITH OR WITHOUT SEBORRHOEA) AND/OR HIRSUTISM, IN WOMEN OF REPRODUCTIVE AGE. FOR THE TREATMENT OF ACNE, CYPRESS SHOULD ONLY BE USED AFTER THERAPY OR SYSTEMIC ANTIBIOTIC TREATMENTS HAVE FAILED |
|---|
| Contraindications | |
|---|
| Side Effects | NAUSEA, ABDOMINAL PAIN, WEIGHT INCREASED, HEADACHE, DEPRESSED MOOD, MOOD ALTERED, BREAST PAIN, BREAST TENDERNESS |
|---|
| Unit Price | |
|---|
| EDL |
No |
|---|
| Description | ROUND, LIGHT PINK, BICONVEX, FILM COATED TABLET DEBOSED " T" ON ONE SIDE AND OTHER SIDE PLAIN |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | MYLAN LABORATORIES LIMITED |
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| Country | INDIA |
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| Import Registration No | G/28/1297 |
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| Import Registration Date | 2016-11-04 |
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| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2022-07-14 |
|---|
| FDD Registration No | 01 I 5665/24 |
|---|
| FDD Registration Date | 2024-01-26 |
|---|
| Expiry Date | 2027-01-25 |
|---|
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